KYGEVVI (DOXECITINE AND DOXRIBTIMINE)
Summary
FDA approved KYGEVVI (DOXECITINE AND DOXRIBTIMINE) by UCB INC. NDA (New Drug) approval (Type 1 - New Molecular Entity) on 2025-11-03. FOR SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
NDA219792-1
Action Date
2025-11-03
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
KYGEVVI (generic: DOXECITINE AND DOXRIBTIMINE), FOR SOLUTION, ORAL. Application: NDA219792
Company
Context & Analysis
UCB INC has 4 FDA actions in our database.
Frequently Asked Questions
How often does UCB INC have FDA actions?
UCB INC has 4 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA219792-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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